Canonical Allele Identifier: CA415259110

Gene: EMD

Linked Data

• MyVariant Identifiers: chrX:g.153609447C>G (hg19) ; chrX:g.154381087C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154381087C>G , CM000685.2:g.154381087C>G	GRCh38
NC_000023.10:g.153609447C>G , CM000685.1:g.153609447C>G	GRCh37
NC_000023.9:g.153262641C>G	NCBI36
NG_008677.1:g.11652C>G , LRG_745:g.11652C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682114.1:c.572+83C>G	ENSP00000507245.1:n.572+83C>G
ENST00000682478.1:n.762+83C>G
ENST00000683576.1:n.845C>G
ENST00000683627.1:c.655C>G	ENSP00000507533.1:p.Gln219Glu
ENST00000684082.1:c.612C>G	ENSP00000508266.1:n.612C>G
ENST00000684633.1:n.627C>G
ENST00000684678.1:c.568+83C>G	ENSP00000507059.1:n.568+83C>G
ENST00000369842.9:c.655C>G MANE Select	ENSP00000358857.4:p.Gln219Glu
ENST00000369835.3:c.550C>G	ENSP00000358850.3:p.Gln184Glu
ENST00000369842.8:c.655C>G	ENSP00000358857.4:p.Gln219Glu
ENST00000428228.5:c.*560C>G	ENSP00000401081.1:n.*560C>G
ENST00000471965.1:n.444C>G
ENST00000486738.5:n.1092C>G
ENST00000492448.1:n.638C>G
NM_000117.2:c.655C>G , LRG_745t1:c.655C>G	NP_000108.1:p.Gln219Glu
XM_024452349.1:c.661C>G	XP_024308117.1:p.Gln221Glu
NM_000117.3:c.655C>G MANE Select	NP_000108.1:p.Gln219Glu